SMP200900055B - Chinazolines for the inhibition of pdk1 - Google Patents
Chinazolines for the inhibition of pdk1Info
- Publication number
- SMP200900055B SMP200900055B SM200900055T SM200900055T SMP200900055B SM P200900055 B SMP200900055 B SM P200900055B SM 200900055 T SM200900055 T SM 200900055T SM 200900055 T SM200900055 T SM 200900055T SM P200900055 B SMP200900055 B SM P200900055B
- Authority
- SM
- San Marino
- Prior art keywords
- chinazolines
- pdk1
- inhibition
- Prior art date
Links
- 101100351314 Caenorhabditis elegans pdk-1 gene Proteins 0.000 title 1
- 125000003790 chinazolinyl group Chemical group 0.000 title 1
- 230000005764 inhibitory process Effects 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/84—Nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/08—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing alicyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Neurology (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Biomedical Technology (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US87697206P | 2006-12-22 | 2006-12-22 | |
US99917007P | 2007-10-15 | 2007-10-15 | |
PCT/US2007/088392 WO2008079988A2 (en) | 2006-12-22 | 2007-12-20 | Quinazolines for pdk1 inhibition |
Publications (2)
Publication Number | Publication Date |
---|---|
SMAP200900055A SMAP200900055A (en) | 2009-09-07 |
SMP200900055B true SMP200900055B (en) | 2010-05-07 |
Family
ID=39563215
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SM200900055T SMP200900055B (en) | 2006-12-22 | 2009-06-30 | Chinazolines for the inhibition of pdk1 |
Country Status (25)
Country | Link |
---|---|
US (1) | US20100216767A1 (en) |
EP (1) | EP2125755A2 (en) |
JP (1) | JP2010514693A (en) |
KR (1) | KR20090092287A (en) |
CN (1) | CN101652352A (en) |
AR (1) | AR065231A1 (en) |
AU (1) | AU2007336893A1 (en) |
BR (1) | BRPI0720563A2 (en) |
CA (1) | CA2673003A1 (en) |
CL (1) | CL2007003774A1 (en) |
CO (1) | CO6361927A2 (en) |
CR (1) | CR10833A (en) |
EA (1) | EA200900819A1 (en) |
EC (1) | ECSP099445A (en) |
IL (1) | IL198774A0 (en) |
MA (1) | MA31001B1 (en) |
MX (1) | MX2009006627A (en) |
NO (1) | NO20092725L (en) |
PE (1) | PE20081630A1 (en) |
SM (1) | SMP200900055B (en) |
SV (1) | SV2009003307A (en) |
TN (1) | TN2009000255A1 (en) |
TW (1) | TW200829558A (en) |
WO (1) | WO2008079988A2 (en) |
ZA (1) | ZA200903233B (en) |
Families Citing this family (62)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UY31137A1 (en) * | 2007-06-14 | 2009-01-05 | Smithkline Beecham Corp | DERIVATIVES OF QUINAZOLINE AS INHIBITORS OF THE PI3 QUINASA |
EP2226315A4 (en) * | 2007-12-28 | 2012-01-25 | Carna Biosciences Inc | 2-aminoquinazoline derivative |
EP2269993B1 (en) * | 2008-04-23 | 2013-02-27 | Kyowa Hakko Kirin Co., Ltd. | 2-aminoquinazoline derivative |
US20100121052A1 (en) * | 2008-06-20 | 2010-05-13 | Rama Jain | Novel compounds for treating proliferative diseases |
WO2010011871A2 (en) * | 2008-07-23 | 2010-01-28 | The Regents Of The University Of California | Methods and compositions for providing salicylic acid-independent pathogen resistance in plants |
EP2330909B1 (en) * | 2008-08-12 | 2013-09-18 | GlaxoSmithKline LLC | Chemical compounds |
EP2381943A1 (en) * | 2008-12-29 | 2011-11-02 | Fovea Pharmaceuticals | Substituted quinazoline compounds |
WO2010092041A1 (en) | 2009-02-13 | 2010-08-19 | Fovea Pharmaceuticals Sa | [1, 2, 4] triazolo [1, 5 -a] pyridines as kinase inhibitors |
GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
TW201204723A (en) | 2010-06-22 | 2012-02-01 | Fovea Pharmaceuticals | Heterocyclic compounds, their preparation and their therapeutic application |
CN101921238B (en) * | 2010-08-04 | 2012-04-04 | 苏州大学附属第一医院 | Preparation of substituted nitrogen-containing benzoheterocycle derivatives and pharmacological application thereof |
GB2497476B (en) | 2010-09-06 | 2018-01-10 | Guangzhou Inst Biomed & Health | Amide Compounds |
EP2632263A1 (en) * | 2010-10-29 | 2013-09-04 | Merck Sharp & Dohme Corp. | Novel thiazole-carboxamide derivatives as pdk1 inhibitors |
DE102010049877A1 (en) | 2010-11-01 | 2012-05-03 | Merck Patent Gmbh | 7 - ((1,2,3) triazol-4-yl) -pyrrolo (2,3) pyrazine derivatives |
KR101902973B1 (en) | 2010-11-24 | 2018-10-04 | 오하이오 스테이트 이노베이션 파운데이션 | Integrin-linked kinase inhibitors |
GB201020179D0 (en) | 2010-11-29 | 2011-01-12 | Astex Therapeutics Ltd | New compounds |
DE102011008352A1 (en) | 2011-01-12 | 2012-07-12 | Merck Patent Gmbh | 5 - ([1,2,3] triazol-4-yl) -7H-pyrrolo [2,3-d] pyrimidine derivatives |
DE102011009961A1 (en) | 2011-02-01 | 2012-08-02 | Merck Patent Gmbh | 7-azaindole derivatives |
PL2762466T3 (en) * | 2011-09-29 | 2017-09-29 | Ono Pharmaceutical Co., Ltd. | Phenyl derivative |
GB201118652D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118656D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118675D0 (en) * | 2011-10-28 | 2011-12-14 | Astex Therapeutics Ltd | New compounds |
GB201118654D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201209609D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
GB201209613D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
RS62233B1 (en) * | 2012-07-11 | 2021-09-30 | Blueprint Medicines Corp | Inhibitors of the fibroblast growth factor receptor |
GB201216018D0 (en) | 2012-09-07 | 2012-10-24 | Cancer Rec Tech Ltd | Pharmacologically active compounds |
GB201216017D0 (en) | 2012-09-07 | 2012-10-24 | Cancer Rec Tech Ltd | Inhibitor compounds |
DE102012019369A1 (en) | 2012-10-02 | 2014-04-03 | Merck Patent Gmbh | 7-Azaindolderivat |
MX2015013618A (en) | 2013-03-26 | 2016-02-25 | Ono Pharmaceutical Co | Phenyl derivative. |
GB201307577D0 (en) | 2013-04-26 | 2013-06-12 | Astex Therapeutics Ltd | New compounds |
CN105636953B (en) | 2013-07-31 | 2018-01-02 | 诺华股份有限公司 | 1,4 dibasic pyridyl derivatives and its purposes for treating the illness related to SMN shortages |
JPWO2015056782A1 (en) * | 2013-10-17 | 2017-03-09 | 塩野義製薬株式会社 | New alkylene derivatives |
ES2930305T3 (en) | 2013-10-18 | 2022-12-09 | Celgene Quanticel Res Inc | Bromodomain inhibitors |
EP3060560A1 (en) | 2013-10-25 | 2016-08-31 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
US9695165B2 (en) | 2014-01-15 | 2017-07-04 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor |
GB201403536D0 (en) | 2014-02-28 | 2014-04-16 | Cancer Rec Tech Ltd | Inhibitor compounds |
JO3512B1 (en) | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | Quinoxaline derivatives useful as fgfr kinase modulators |
HUE053654T2 (en) | 2014-03-26 | 2021-07-28 | Astex Therapeutics Ltd | Combinations of fgfr- and cmet-inhibitors for the treatment of cancer |
BR112016022062B1 (en) | 2014-03-26 | 2023-04-11 | Astex Therapeutics Limited | COMBINATION, PHARMACEUTICAL COMPOSITION, USE OF A COMBINATION OR A PHARMACEUTICAL COMPOSITION, AND, PHARMACEUTICAL PRODUCT |
JOP20200201A1 (en) | 2015-02-10 | 2017-06-16 | Astex Therapeutics Ltd | Pharmaceutical compositions comprising n-(3,5-dimethoxyphenyl)-n'-(1-methylethyl)-n-[3-(1-methyl-1h-pyrazol-4-yl)quinoxalin-6-yl]ethane-1,2-diamine |
EP3263714B1 (en) * | 2015-02-24 | 2021-08-25 | Theoria Science Inc. | Method for diagnosing brain metastasis |
US10478494B2 (en) | 2015-04-03 | 2019-11-19 | Astex Therapeutics Ltd | FGFR/PD-1 combination therapy for the treatment of cancer |
CA2992945A1 (en) | 2015-07-17 | 2017-01-26 | Memorial Sloan-Kettering Cancer Center | Combination therapy using pdk1 and pi3k inhibitors |
HRP20220012T1 (en) | 2015-09-23 | 2022-04-01 | Janssen Pharmaceutica Nv | Bi-heteroaryl substituted 1,4-benzodiazepines and uses thereof for the treatment of cancer |
CA2996857C (en) | 2015-09-23 | 2024-05-21 | Janssen Pharmaceutica Nv | Quinoxaline, quinoline and quinazolinone derivative compounds for the treatment of cancer |
EP3356348B1 (en) | 2015-10-02 | 2021-05-05 | Sentinel Oncology Limited | 2-aminoquinazoline derivatives as p70s6 kinase inhibitors |
GB201705263D0 (en) * | 2017-03-31 | 2017-05-17 | Probiodrug Ag | Novel inhibitors |
GB201709840D0 (en) | 2017-06-20 | 2017-08-02 | Inst Of Cancer Research: Royal Cancer Hospital | Methods and medical uses |
BR112020005489A2 (en) | 2017-09-22 | 2020-09-24 | Jubilant Epipad Llc, | compound of formula (i), compound of formula (ii), compound of formula (iii), process of preparing compounds of formula (i), process of preparing compounds of formula (ii), process of preparing compounds of formula (iii), pharmaceutical composition, method for inhibiting one or more pad families in a cell, method for treating a condition mediated by one or more pads, use of the compound, method for treating and / or preventing a condition mediated by one or more more disorders of the pad family, method for treating rheumatoid arthritis and cancer treatment method |
PT3697785T (en) | 2017-10-18 | 2023-04-03 | Jubilant Epipad LLC | Imidazo-pyridine compounds as pad inhibitors |
BR112020008851A2 (en) | 2017-11-06 | 2020-10-20 | Jubilant Prodel LLC | compound of formula i, process for preparing compounds of formula i, pharmaceutical composition, method for treating and / or preventing various diseases, use, method for treating cancer, method of treating cancer and method for treating and / or prevention of cancer and infectious diseases |
JP7368369B2 (en) | 2017-11-24 | 2023-10-24 | ジュビラント・エピスクライブ・エルエルシー | Heterocyclic compounds as PRMT5 inhibitors |
WO2019175897A1 (en) | 2018-03-13 | 2019-09-19 | Jubilant Biosys Limited | Bicyclic compounds as inhibitors of pd1/pd-l1 interaction/activation |
CN114315798A (en) * | 2020-09-29 | 2022-04-12 | 深圳智药信息科技有限公司 | Quinazoline compound and pharmaceutical composition thereof |
CN117024445A (en) * | 2020-10-28 | 2023-11-10 | 杭州阿诺生物医药科技有限公司 | Compounds for preparing HPK1 kinase inhibitor and synthesis method thereof |
CN114533733A (en) * | 2021-12-31 | 2022-05-27 | 北京鑫开元医药科技有限公司 | Isoquinoline-1, 3-diamine analogue pharmaceutical preparation and preparation method thereof |
CN113999206B (en) * | 2021-12-31 | 2022-04-12 | 北京鑫开元医药科技有限公司 | Isoquinoline-1, 3-diamine analogue, preparation method, pharmaceutical composition and application thereof |
WO2023138412A1 (en) * | 2022-01-20 | 2023-07-27 | Insilico Medicine Ip Limited | Fused pyrimidin-2-amine compounds as cdk20 inhibitors |
TW202345806A (en) | 2022-03-31 | 2023-12-01 | 美商艾伯維有限公司 | Thiazolo[5,4-b]pyridine malt-1 inhibitors |
WO2023218241A1 (en) * | 2022-05-13 | 2023-11-16 | Voronoi Inc. | Heteroaryl derivative compounds, and pharmaceutical composition comprising thereof |
WO2024131938A1 (en) * | 2022-12-23 | 2024-06-27 | 赛诺哈勃药业(成都)有限公司 | Quinazoline compound and use thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5079500B2 (en) * | 2005-04-28 | 2012-11-21 | 協和発酵キリン株式会社 | 2-Aminoquinazoline derivatives |
TW200808739A (en) * | 2006-04-06 | 2008-02-16 | Novartis Vaccines & Diagnostic | Quinazolines for PDK1 inhibition |
WO2008020203A1 (en) * | 2006-08-17 | 2008-02-21 | Astrazeneca Ab | Pyridinylquinaz0linamine derivatives and their use as b-raf inhibitors |
TW200829566A (en) * | 2006-12-08 | 2008-07-16 | Astrazeneca Ab | Chemical compounds |
-
2007
- 2007-12-20 MX MX2009006627A patent/MX2009006627A/en not_active Application Discontinuation
- 2007-12-20 EA EA200900819A patent/EA200900819A1/en unknown
- 2007-12-20 BR BRPI0720563-5A patent/BRPI0720563A2/en not_active IP Right Cessation
- 2007-12-20 US US12/448,390 patent/US20100216767A1/en not_active Abandoned
- 2007-12-20 CA CA002673003A patent/CA2673003A1/en not_active Abandoned
- 2007-12-20 CN CN200780047581A patent/CN101652352A/en active Pending
- 2007-12-20 WO PCT/US2007/088392 patent/WO2008079988A2/en active Application Filing
- 2007-12-20 JP JP2009543225A patent/JP2010514693A/en not_active Withdrawn
- 2007-12-20 AU AU2007336893A patent/AU2007336893A1/en not_active Abandoned
- 2007-12-20 KR KR1020097012780A patent/KR20090092287A/en not_active Application Discontinuation
- 2007-12-20 EP EP07869660A patent/EP2125755A2/en not_active Withdrawn
- 2007-12-21 TW TW096149570A patent/TW200829558A/en unknown
- 2007-12-21 AR ARP070105879A patent/AR065231A1/en unknown
- 2007-12-21 CL CL200703774A patent/CL2007003774A1/en unknown
-
2008
- 2008-01-02 PE PE2008000067A patent/PE20081630A1/en not_active Application Discontinuation
-
2009
- 2009-05-11 ZA ZA200903233A patent/ZA200903233B/en unknown
- 2009-05-14 IL IL198774A patent/IL198774A0/en unknown
- 2009-05-28 CR CR10833A patent/CR10833A/en not_active Application Discontinuation
- 2009-06-17 MA MA32005A patent/MA31001B1/en unknown
- 2009-06-17 CO CO09062868A patent/CO6361927A2/en not_active Application Discontinuation
- 2009-06-19 EC EC2009009445A patent/ECSP099445A/en unknown
- 2009-06-19 TN TNP2009000255A patent/TN2009000255A1/en unknown
- 2009-06-19 SV SV2009003307A patent/SV2009003307A/en not_active Application Discontinuation
- 2009-06-30 SM SM200900055T patent/SMP200900055B/en unknown
- 2009-07-17 NO NO20092725A patent/NO20092725L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
ZA200903233B (en) | 2010-04-28 |
WO2008079988A3 (en) | 2008-10-16 |
MA31001B1 (en) | 2009-12-01 |
WO2008079988A2 (en) | 2008-07-03 |
IL198774A0 (en) | 2010-02-17 |
AR065231A1 (en) | 2009-05-27 |
ECSP099445A (en) | 2009-07-31 |
SMAP200900055A (en) | 2009-09-07 |
EA200900819A1 (en) | 2010-02-26 |
TN2009000255A1 (en) | 2010-10-18 |
BRPI0720563A2 (en) | 2014-02-04 |
SV2009003307A (en) | 2010-05-21 |
AU2007336893A1 (en) | 2008-07-03 |
CN101652352A (en) | 2010-02-17 |
NO20092725L (en) | 2009-09-22 |
CA2673003A1 (en) | 2008-07-03 |
US20100216767A1 (en) | 2010-08-26 |
WO2008079988A9 (en) | 2011-05-12 |
JP2010514693A (en) | 2010-05-06 |
MX2009006627A (en) | 2009-08-12 |
EP2125755A2 (en) | 2009-12-02 |
TW200829558A (en) | 2008-07-16 |
PE20081630A1 (en) | 2008-12-14 |
CO6361927A2 (en) | 2012-01-20 |
KR20090092287A (en) | 2009-08-31 |
CL2007003774A1 (en) | 2008-04-18 |
CR10833A (en) | 2009-07-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SMP200900055B (en) | Chinazolines for the inhibition of pdk1 | |
SMAP200800059A (en) | Chinazolines for the inhibition of pdk1 | |
BRPI0719626A2 (en) | '' COMPOUND '' | |
ZA200705783B (en) | Amino-imidazolones for the inhibition of ß-secretase | |
BRPI0922904A2 (en) | "compounds" | |
IL189933A0 (en) | Rna antagonist compounds for the inhibition of apo-b100 expression | |
SMAP200900085A (en) | 3-imidazolyl-indoles for the treatment of malolysiseproliferative | |
ZA200903401B (en) | The uses of the carboxy-amido-triazole compounds and salts thereof | |
ZA200902808B (en) | An alzheimer's disease progression inhibitor containing heterocyclic compound having specific structure | |
ITMI20061848A1 (en) | PROCEDURE FOR THE PREPARATION OF PHENYLTETRAZOLIC COMPOUNDS | |
BRPI0819546A2 (en) | "capacitor" | |
ITPD20060400A1 (en) | "MUFFLE STRUCTURE" | |
AT505229A3 (en) | POTENTIAL HELP '' PENISSCHLAUCH '' | |
ITMI20060489A1 (en) | PROCEDURE FOR THE PREPARATION OF 1-BEONO-3-TRIFLUOROMETOSSIBENZENE | |
IT1367578B1 (en) | EQUIPMENT FOR ORIENTATION OF ITEMS | |
FR2895710B1 (en) | MONOPODE OF ARRIMAGE FOR BRANCARD | |
FR2897520B3 (en) | USTENSILE OF ASSUJETMENT OF OBJECTS | |
ES1062999Y (en) | "SELF-CONFORMABLE BOX-CASE" | |
ITVB20060005U1 (en) | "VIBROLO" | |
ITMO20060346A1 (en) | "COLLIRIO SOAP" | |
UA15331S (en) | NOTE | |
UA17706S (en) | SET OF CONNECTED CONTAINERS | |
UA17705S (en) | SET OF CONNECTED CONTAINERS | |
ITVR20080023U1 (en) | THE SET OF TENUTA TATAMI | |
ITCT20070008U1 (en) | "DOCCIASCIUGA" |